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rs193922420

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922420(A;A)
Make rs193922420(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position122254295
GeneCASR
is asnp
is mentioned by
dbSNPrs193922420
dbSNP (classic)rs193922420
ClinGenrs193922420
ebirs193922420
HLIrs193922420
Exacrs193922420
Gnomadrs193922420
Varsomers193922420
LitVarrs193922420
Maprs193922420
PheGenIrs193922420
Biobankrs193922420
1000 genomesrs193922420
hgdprs193922420
ensemblrs193922420
geneviewrs193922420
scholarrs193922420
googlers193922420
pharmgkbrs193922420
gwascentralrs193922420
openSNPrs193922420
23andMers193922420
SNPshotrs193922420
SNPdbers193922420
MSV3drs193922420
GWAS Ctlgrs193922420
Max Magnitude0
ClinVar
Risk rs193922420(A;A)
Alt rs193922420(A;A)
Reference Rs193922420(G;G)
Significance Probable-Pathogenic
Disease Familial hypocalciuric hypercalcemia not specified
Variation info
Gene CASR
CLNDBN Familial hypocalciuric hypercalcemia not specified
Reversed 0
HGVS NC_000003.11:g.121973142G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029426.1, RCV000341520.1,